LAT1 (SLC7A5) Overexpression in Negative Her2 Group of Breast Cancer: A Potential Therapy Target
Language English Country Thailand Media electronic
Document type Journal Article
PubMed
32458655
PubMed Central
PMC7541863
DOI
10.31557/apjcp.2020.21.5.1453
PII: 89076
Knihovny.cz E-resources
- Keywords
- HER2, LAT1, SLC7A5, breast cancer,
- MeSH
- Adult MeSH
- Carcinoma, Ductal, Breast metabolism pathology surgery MeSH
- Neoplasm Invasiveness MeSH
- Middle Aged MeSH
- Humans MeSH
- Carcinoma, Lobular metabolism pathology surgery MeSH
- Neoplasm Recurrence, Local metabolism pathology surgery MeSH
- Lymphatic Metastasis MeSH
- Survival Rate MeSH
- Biomarkers, Tumor metabolism MeSH
- Follow-Up Studies MeSH
- Large Neutral Amino Acid-Transporter 1 metabolism MeSH
- Prognosis MeSH
- Receptor, ErbB-2 metabolism MeSH
- Receptors, Estrogen metabolism MeSH
- Receptors, Progesterone metabolism MeSH
- Gene Expression Regulation, Neoplastic MeSH
- Retrospective Studies MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Triple Negative Breast Neoplasms metabolism pathology surgery MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Aged, 80 and over MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- ERBB2 protein, human MeSH Browser
- Biomarkers, Tumor MeSH
- Large Neutral Amino Acid-Transporter 1 MeSH
- Receptor, ErbB-2 MeSH
- Receptors, Estrogen MeSH
- Receptors, Progesterone MeSH
- SLC7A5 protein, human MeSH Browser
OBJECTIVE: HER2 negative carcinomas of the breast pose a challenge for treatment due to redundancies in potential drug targets and poor patient outcomes. Our aim was to investigate the role of L-type amino acid transporter - LAT1 as a potential prognosticator and a drug target. METHODS: In this retrospective work, we have studied the expression of LAT1 in 145 breast cancer tissues via immunohistochemistry. Overall survival analysis was used to evaluate patient outcome in various groups of our cohort. RESULTS: Positive LAT1 expression was found in 27 (84.4%) luminal A subtype, 27 (64.3%) luminal B/triple positive subtype, 29 (82.9%) triple negative subtype, and 24 (66.7%) HER2-only positive subtype (p=0.1). Interestingly, negative correlation was found between LAT1 and HER2; where positive expression of LAT1 was found in 56 (83.6%) cases in negative HER2 group and 51 (65.4%) cases from positive HER2 group (p=0.01). Unfortunately, we were unable to report significant survival differences when LAT1 expression was studied in the negative HER2 group. Nevertheless, five incidents of mortality (out of 55) were reported in LAT1+/HER2- group compared to none in the LAT1-/HER2- group (N=11). CONCLUSION: Our findings of overexpression of LAT1 in negative HER2 group suggest a role of this protein as prognosticator and drug target in a challenging therapeutic cohort.
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Central European Institute of Technology Brno University of Technology Purkynova Brno Czech Republic
Department of Applied Biology Jordan University of Science and Technology Irbid Jordan
Department of Chemistry and Biochemistry Mendel University in Brno Zemedelska 1 Brno Czech Republic
Department of Medical Laboratory Sciences Jordan University of Science and Technology Irbid Jordan
Department of Pathology Jordan University of Science and Technology Irbid Jordan
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